The i-gel® supraglottic airway device compared to endotracheal intubation as the initial prehospital advanced airway device : A natural experiment during the COVID-19 pandemic

© 2024 The Authors. Journal of the American College of Emergency Physicians Open published by Wiley Periodicals LLC on behalf of American College of Emergency Physicians..

Objective: Unlike randomized controlled trials, practical real-world studies can offer important information about implementation of prehospital interventions, particularly in community settings where there may be reluctance to adopt new practices. We present the results of a natural experiment that was driven by mandated COVID-19 pandemic-driven shift from endotracheal intubation (ETI) to the i-gel® supraglottic airway (SGA) as a primary advanced airway management device in the prehospital setting to reduce emergency medical services (EMS) personnel exposure to potentially infectious secretions. The objective was to compare first-pass success and timing to successful airway placement between ETI and the i-gel® SGA under extenuating circumstances.

Methods: This pre/post study compared airway placement metrics in prehospital patients requiring advance airway management for non-trauma-related conditions. Data from EMS records were extracted over 2 years, 12 months pre-pandemic, and 12 months post-pandemic. During the pre-COVID-19 year, the EMS protocols utilized ETI as the primary advanced airway device (ETI group). Post-pandemic paramedics were mandated to utilize i-gel® SGA as the primary advanced airway device to reduce exposure to secretions (SGA group).

Results: There were 199 adult patients, 83 (42%) in the ETI group and 116 (58%) in the SGA group. First-pass success was significantly higher with SGA 96% (92%-99%) than ETI 68% (57%-78%) with paramedics citing the inability to visualize the airway in 52% of ETI cases. Time to first-pass success was significantly shorter in the SGA group (5.9 min [5.1-6.7 min]) than in the ETI group (8.3 min [6.9-9.6 min]), as was time to overall successful placement at 6.0 min (5.1-6.8 min) versus 9.6 min (8.2-11.1 min), respectively. Multiple placement attempts were required in 26% of ETI cases and 1% of the SGA cases. There were no statistically significant differences in the number and types of complications between the cohorts. Return of spontaneous circulation (on/before emergency department [ED] arrival), mortality at 28 days, intensive care unit length of stay, or ventilator-free days between the groups were not statistically different between the groups.

Conclusion: In this natural experiment, the SGA performed significantly better than ETI in first-pass airway device placement success and was significantly faster in achieving first-pass success, and overall airway placement, thus potentially reducing exposure to respiratory pathogens. Practical real-world studies can offer important information about implementation of prehospital interventions, particularly in community settings and in systems with a low frequency of tracheal intubations.

Medienart:

E-Artikel

Erscheinungsjahr:

2024

Erschienen:

2024

Enthalten in:

Zur Gesamtaufnahme - volume:5

Enthalten in:

Journal of the American College of Emergency Physicians open - 5(2024), 2 vom: 24. Apr., Seite e13150

Sprache:

Englisch

Beteiligte Personen:

Levi, Daniel [VerfasserIn]
Hoogendoorn, Joris [VerfasserIn]
Samuels, Shenae [VerfasserIn]
Maguire, Lindsay [VerfasserIn]
Troncoso, Ruben [VerfasserIn]
Gunn, Scott [VerfasserIn]
Katz, Matthew [VerfasserIn]
VanDillen, Christine [VerfasserIn]
Miller, Susan A [VerfasserIn]
Falk, Jay L [VerfasserIn]
Katz, Steven H [VerfasserIn]
Papa, Linda [VerfasserIn]

Links:

Volltext

Themen:

Airway
COVID‐19
Emergency medical services
Endotracheal intubation
ICU length of stay
Journal Article
Mortality
Out‐of‐hospital cardiac arrest
Pandemic
Paramedics
Prehospital
Return of spontaneous circulation
Supraglottic airway
Ventilator‐free days

Anmerkungen:

Date Revised 06.04.2024

published: Electronic-eCollection

Citation Status PubMed-not-MEDLINE

doi:

10.1002/emp2.13150

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM370660234